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Abstract #1257

The impact of amyloid-β and ferritin on ultra-high-field R2* and quantitative susceptibility mapping

Jierong Luo1, James Everett2, Jane Donnelly1,3, Festus Slade1,4,5, Neil Telling2, and Joanna F Collingwood1,5
1School of Engineering, University of Warwick, Coventry, United Kingdom, 2School of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent, United Kingdom, 3Feinberg School of Medicine, Northwestern University, Chicago, IL, United States, 4Department of Chemistry, University of Warwick, Coventry, United Kingdom, 5Warwick Centre for Doctoral Training in Analytical Science, University of Warwick, Coventry, United Kingdom

Synopsis

Keywords: Quantitative Imaging, Contrast Mechanisms, MR Microscopy, Quantitative Susceptibility Mapping, R2*, Iron, Ferritin, Amyloid plaques, Alzheimer's Disease

Amyloid plaques, an established hallmark of Alzheimer's disease, are often demonstrably associated with iron deposits post-mortem. Previous T2*-weighted and phase information from ultra-high-field MR microscopy and clinical MRI has shown the potential to detect amyloid deposits in vivo and ex vivo. We investigated the relative contributions to contrast from amyloid-β (Aβ) aggregates with and without ferritin-bound iron in vitro, for R2* and quantitative susceptibility maps (QSM) with 86 μm isotropic resolution at 9.4T. We also demonstrated the quantitative signal evolution with the formation of amyloid aggregates, and the correlation of the signals with the Aβ and ferritin content.

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